Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16550 | A02 | 8094623 | G | A | synonymous_variant | LOW | c.1908C>T|p.Val636Val |
S223 |
2 | BAA02g16550 | A02 | 8094668 | C | T | synonymous_variant | LOW | c.1863G>A|p.Lys621Lys |
S38 |
3 | BAA02g16550 | A02 | 8094884 | C | T | stop_gained | HIGH | c.1647G>A|p.Trp549* |
S250 |
4 | BAA02g16550 | A02 | 8095447 | C | T | missense_variant | MODERATE | c.1084G>A|p.Asp362Asn |
S72 S78 |
5 | BAA02g16550 | A02 | 8095600 | T | G | missense_variant | MODERATE | c.931A>C|p.Lys311Gln |
S163 S7 S90 |
6 | BAA02g16550 | A02 | 8095882 | G | A | missense_variant | MODERATE | c.649C>T|p.Pro217Ser |
S69 |
7 | BAA02g16550 | A02 | 8096119 | C | T | missense_variant | MODERATE | c.488G>A|p.Ser163Asn |
S180 |
8 | BAA02g16550 | A02 | 8096956 | G | A | stop_gained | HIGH | c.61C>T|p.Gln21* |
S166 |
9 | BAA02g16550 | A02 | 8097285 | C | T | upstream_gene_variant | MODIFIER | c.-269G>A| |
S125 S162 S178 |
10 | BAA02g16550 | A02 | 8100536 | G | A | upstream_gene_variant | MODIFIER | c.-3520C>T| |
S150 |